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Alliance of Genome Resources

Alliance of Genome Resources is a gene dataset, which contains curated genome information essential for the understanding of the genetics and genomic basis of human biology, health and disease. All data is retrieved from six major model organism databases and the Gene Ontology including FlyBase, Mouse Genome Database (MGI), Rat Genome Database (RGD), Saccharomyces Genome Database (SGD), WormBase, Zebrafish Information Network (ZFIN), and the GO Consortium. In GlyCosmos, only glycan-related disease information has been extracted from Alliance of Genome Resources.

Source Last Updated
Alliance of Genome Resources July 29, 2024
Displaying entries 9926 - 9950 of 12216 in total
Disease ID Disease Name Alliance of Genome Resources ID Species Gene ID ▲ Gene Symbol FlyGlycoDB Evidence Code Names References
DOID:0050861 colorectal adenocarcinoma HGNC:1097 Homo sapiens (human) 673 BRAF
  • PMID:24500602
DOID:0050700 cardiomyopathy HGNC:1097 Homo sapiens (human) 673 BRAF
  • MGI:6194238
DOID:12858 Huntington's disease MGI:1914625 Mus musculus (house mouse) 67375 Qprt
  • MGI:6194238
DOID:0080470 developmental and epileptic encephalopathy 36 MGI:1914824 Mus musculus (house mouse) 67574 Alg13
  • MGI:6194238
DOID:0080208 metabolic dysfunction-associated steatotic liver disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:10787 premature menopause MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:9452 steatotic liver disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:784 chronic kidney disease MGI:1915050 Mus musculus (house mouse) 67800 Dgat2
  • MGI:6194238
DOID:1380 endometrial cancer HGNC:11377 Homo sapiens (human) 6783 SULT1E1
  • PMID:18318428
DOID:1612 breast cancer HGNC:11377 Homo sapiens (human) 6783 SULT1E1
  • PMID:15894657
  • PMID:17372239
DOID:2566 corneal dystrophy HGNC:14415 Homo sapiens (human) 6785 ELOVL4
  • PMID:11726641
DOID:0050817 Stargardt disease HGNC:14415 Homo sapiens (human) 6785 ELOVL4
  • MGI:6194238
DOID:0050981 spinocerebellar ataxia type 34 HGNC:14415 Homo sapiens (human) 6785 ELOVL4
  • RGD:7240710
DOID:0050773 paraganglioma MGI:1915113 Mus musculus (house mouse) 67863 Slc25a11
  • MGI:6194238
DOID:0111258 pentosuria MGI:1915130 Mus musculus (house mouse) 67880 Dcxr
  • MGI:6194238
DOID:9970 obesity MGI:1915304 Mus musculus (house mouse) 68054 Serpina12
  • MGI:6194238
DOID:9352 type 2 diabetes mellitus MGI:1915304 Mus musculus (house mouse) 68054 Serpina12
  • MGI:6194238
DOID:0080258 autosomal recessive congenital ichthyosis 14 HGNC:11459 Homo sapiens (human) 6820 SULT2B1
  • RGD:7240710
DOID:2841 asthma MGI:1915464 Mus musculus (house mouse) 68214 Gsto2
  • MGI:6194238
DOID:10652 Alzheimer's disease MGI:1915464 Mus musculus (house mouse) 68214 Gsto2
  • MGI:6194238
DOID:1574 alcohol use disorder MGI:1915464 Mus musculus (house mouse) 68214 Gsto2
  • MGI:6194238
DOID:14330 Parkinson's disease MGI:1915464 Mus musculus (house mouse) 68214 Gsto2
  • MGI:6194238
DOID:3649 pyruvate decarboxylase deficiency MGI:1915513 Mus musculus (house mouse) 68263 Pdhb
  • MGI:6194238
DOID:0110292 autosomal recessive limb-girdle muscular dystrophy type 2O MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238
DOID:0050453 lissencephaly MGI:1915523 Mus musculus (house mouse) 68273 Pomgnt1
  • MGI:6194238

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GlyCosmos is a member of the GlySpace Alliance together with GlyGen and Glycomics@ExPASy.

Acknowledgements

Supported by JST NBDC Grant Number JPMJND2204

Partly supported by NIH Common Fund Grant #1U01GM125267-01


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Last updated: August 19, 2024